Lee Tsong-Hai, Cheng Mei-Ling, Shiao Ming-Shi, Lin Chia-Ni
Stroke Center and Department of Neurology, Linkou Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Department of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
BMC Neurol. 2019 Jun 24;19(1):138. doi: 10.1186/s12883-019-1371-x.
Significant genetic association has been found in patients with severe carotid artery stenosis (CAS). The present study wished to investigate if metabolites may also act as biomarkers for CAS.
Consecutive patients with at least one carotid artery stenosis > = 60% on cerebral angiography were prospectively recruited from May 2007 to January 2016. Normal controls were recruited from outpatient clinic who had no stroke and coronary artery disease (CAD) history, and the brain magnetic resonance or computed tomographic angiography showed bilateral CAS < 30%. Risk factor profile, clinical characteristics, age, and clinical features were recorded. All subjects were male, and none had diabetes. H-NMR spectroscopy-based metabolomics analysis was carried out for plasma samples.
Totally, 130 male subjects were recruited. Age had no significant difference between the controls and CAS group (60.2 ± 5.9 vs. 63.3 ± 6.0, p = 0.050). The CAS group had significantly higher frequency of CAD, hypertension, smoking and alcohol but lower body mass index than the controls (p < 0.05). The laboratory tests showed CAS group had significantly higher level of homocysteine but lower levels of cholesterol, high-density lipoprotein and hemoglobin than the controls (p < 0.05). The H-NMR based plasma metabolomics analysis indicated that choline was significantly lower in CAS patients. The VIP values of lipids were greater than 1.0, which were considered significantly different.
Our results suggest homocysteine, choline and lipids in association with traditional risk factors may be involved in the pathogenesis of CAS. Diet adjustment to control homocysteine, choline and lipids may be helpful for the prevention of CAS.
在重度颈动脉狭窄(CAS)患者中已发现显著的基因关联。本研究旨在调查代谢物是否也可作为CAS的生物标志物。
从2007年5月至2016年1月前瞻性招募连续的在脑血管造影中至少有一处颈动脉狭窄≥60%的患者。正常对照从无卒中及冠状动脉疾病(CAD)病史的门诊患者中招募,且脑磁共振或计算机断层血管造影显示双侧CAS<30%。记录危险因素概况、临床特征、年龄及临床表现。所有受试者均为男性,且均无糖尿病。对血浆样本进行基于氢核磁共振波谱的代谢组学分析。
共招募了130名男性受试者。对照组与CAS组之间年龄无显著差异(60.2±5.9对63.3±6.0,p = 0.050)。与对照组相比,CAS组CAD、高血压、吸烟及饮酒的发生率显著更高,但体重指数更低(p<0.05)。实验室检查显示,CAS组同型半胱氨酸水平显著更高,但胆固醇、高密度脂蛋白及血红蛋白水平低于对照组(p<0.05)。基于氢核磁共振波谱法的血浆代谢组学分析表明,CAS患者的胆碱显著更低。脂质的VIP值大于1.0,被认为有显著差异。
我们的结果表明,同型半胱氨酸、胆碱及脂质与传统危险因素相关,可能参与了CAS的发病机制。通过饮食调整来控制同型半胱氨酸、胆碱及脂质可能有助于预防CAS。